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3. Identification of new markers in Xp21 between DXS28 (C7) and DMD. Worley KC; Towbin JA; Zhu XM; Barker DF; Ballabio A; Chamberlain J; Biesecker LG; Blethen SL; Brosnan P; Fox JE Genomics; 1992 Aug; 13(4):957-61. PubMed ID: 1505987 [TBL] [Abstract][Full Text] [Related]
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9. Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell lines. Francis F; Benham F; See CG; Fox M; Ishikawa-Brush Y; Monaco AP; Weiss B; Rappold G; Hamvas RM; Lehrach H Genomics; 1994 Mar; 20(1):75-83. PubMed ID: 8020959 [TBL] [Abstract][Full Text] [Related]
10. Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus. Towbin JA; Wu DR; Chamberlain J; Larsen PD; Seltzer WK; McCabe ER Hum Genet; 1989 Sep; 83(2):122-6. PubMed ID: 2550352 [TBL] [Abstract][Full Text] [Related]
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12. Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia. Marlhens F; Chelly J; Kaplan JC; Lefrancois D; Harpey JP; Dutrillaux B Hum Genet; 1987 Dec; 77(4):379-83. PubMed ID: 2891606 [TBL] [Abstract][Full Text] [Related]
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